Product Recalls in Arkansas
Product recalls affecting Arkansas — including food, drugs, consumer products, medical devices, and vehicles distributed to Arkansas. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,614 recalls have been distributed to Arkansas in the last 12 months.
Showing 12541–12560 of 49,990 recalls
Recalled Item: Sensis Recalled by Siemens Medical Solutions USA, Inc Due to Siemens has...
The Issue: Siemens has become aware of three potential software issues with AXIOM...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AUTOLITH Touch 1.9F 375cm Biliary Electrohydraulic Lithotripter Probe...
The Issue: Product labeled incorrectly.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Getinge CM320-2 CHAMBER WU Series Washer Disinfector- For Use as Recalled by...
The Issue: Verification of installation not documented or may be incomplete, could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Insulin Glargine (insulin glargine-yfgn) Injection Recalled by Mylan...
The Issue: Labeling: Missing label on the vial
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Losartan Potassium Tab. USP 50mg Recalled by Preferred Pharmaceuticals, Inc....
The Issue: CGMP Deviations- AZIDO Impurity levels observed to be above acceptable limits.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Crome Models loaded with CareLink SmartSync Device Manager application...
The Issue: Telemetry error that may occur with Medtronic Cobalt and Crome implantable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cobalt Models loaded with CareLink SmartSync Device Manager application...
The Issue: Telemetry error that may occur with Medtronic Cobalt and Crome implantable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pantoprazole Sodium Delayed-Release Tablets Recalled by Torrent Pharma Inc...
The Issue: CGMP deviations: tablets cracking
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Artis icono biplane -angiography systems developed for single and biplane...
The Issue: if the protective earth is interrupted and an additional fault leads to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis icono floor-angiography systems developed for single and biplane...
The Issue: if the protective earth is interrupted and an additional fault leads to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AC-powered adjustable medical beds with built-in electric DC actuators and...
The Issue: There is a potential hazard of uninterrupted motion of the Motorized Wheel...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AC-powered adjustable medical beds with built-in electric DC actuators and...
The Issue: There is a potential hazard of uninterrupted motion of the Motorized Wheel...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: (1) Gibeck Humid-Vent 2S Flex DC Recalled by TELEFLEX MEDICAL INC Due to...
The Issue: Reports received of torn corrugated breathing tubes.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: (1) Teleflex Flex tube Recalled by TELEFLEX MEDICAL INC Due to Reports...
The Issue: Reports received of torn corrugated breathing tubes.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Radiometer Recalled by Radiometer Medical ApS Due to Arterial Blood Sampler...
The Issue: Arterial Blood Sampler sterility cannot be guaranteed throughout the shelf...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HemosIL ReadiPlasTin Recalled by Instrumentation Laboratory Due to Variable...
The Issue: Variable and out of specification QC results with HemosIL ReadiPlasTin. IL...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TMJ Arthroscopy Drape Recalled by Microtek Medical Inc. Due to Latex content...
The Issue: Latex content in product was labeled incorrectly as latex free.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Rifampin for Injection Recalled by Mylan Pharmaceuticals Inc Due to Failed...
The Issue: Failed Impurities/Degradation Specifications: High out of specification...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: NanoSight NS300 Recalled by MALVERN PANALYTICAL LTD Due to Product found to...
The Issue: Product found to not comply to Class 1 Laser safety requirement.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Resin UPDATE CD-ROM Recalled by Bio-Rad Laboratories, Inc. Due to The...
The Issue: The problem is with the Bio-Rad VARIANT nbs Sickle Cell Program Resin Update...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.